Disease #00140 (KEFH (KERATOENDOTHELIITIS FUGAX HEREDITARIA), OMIM:148200)
Official abbreviation |
KEFH |
Name |
KERATOENDOTHELIITIS FUGAX HEREDITARIA |
OMIM ID |
148200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
NLRP3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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